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The Francis Crick Papers

Letter from H. Gobind Khorana to Francis Crick pdf (270,220 Bytes) transcript of pdf
Letter from H. Gobind Khorana to Francis Crick
In this letter Khorana reported on recent work in his laboratory on alanine tRNA in yeast and in the bacterium E-coli, as well as on the TAG codon in DNA, which becomes UAG during transcription into RNA and which codes for the termination of a polypeptide chain.
The "commotion of last fall" mentioned in the first paragraph referred to the award of a share of the 1968 Nobel Prize to Khorana.
Item is handwritten.
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1 (270,220 Bytes)
1969-04-12 (April 12, 1969)
Khorana, H. Gobind
Crick, Francis
Original Repository: Wellcome Library for the History and Understanding of Medicine. Francis Harry Compton Crick Papers
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Reproduced with permission of H. Gobind Khorana.
Medical Subject Headings (MeSH):
Genetic Code
Exhibit Category:
Embryology and the Organization of DNA in Higher Organisms, 1966-1976
Metadata Record Letter from Francis Crick to H. Gobind Khorana (April 16, 1969) pdf (53,714 Bytes) transcript of pdf
Metadata Record Letter from Francis Crick to H. Gobind Khorana (March 6, 1969) pdf (121,243 Bytes) transcript of pdf
Box Number: 9
Folder Number: PP/CRI/D/1/1/11
Unique Identifier:
Document Type:
Letters (correspondence)
Physical Condition:
Series: Correspondence
SubSeries: Alphabetical Correspondence
SubSubSeries: Correspondence 1
Folder: Correspondence K
April 12, 69.
Dr. F.H.C. Crick FRS
Dear Francis,
I was happy to receive your letter about a month ago. I am sorry for the delay -- Actually I found my commitments to West Coast this year in Feb. and the commotion of last fall all very trying. On returning from West Coast I came down with nervous exhaustion. I am feeling a bit better now and am soon leaving for Switzerland for a several weeks vacation.
Regarding your two points
(1) Ala-tRNA sequence. We ourselves had been worrying a lot about correctness of sequence around A-G (in so-called di-Hydro U region) and also as you may have seen, Carl Merril (Biopolymers, 6, 1727 (1968)) wants to add another G unit in the structure.
I have decided not to worry about these. The main aims at this stage as far as our synthetic work on yeast ala tRNA are (1) to work out the total chem.-enzymatic methodology for construction and characterization of DNA duplexes. (2) to learn to multiply these with DNA polymerase (3) to learn to transcribe the actual structure -- function, alliolionis [?] of gene etc etc will all be done (Whenever in the next decade (?) we get to it) with the E. coli tRNA gene which, as you know, we have also started on.
(2) Regarding UAG polymer -- What with turn-over of people and loss of my interest in repeating polymers, I find it difficult to maintain adequate checks and stocks on these. But, we could arrange to send informational amount of the DNA-polymer. Your people would have to multiply and then transcribe etc etc.
(3) Lastly Bob Bock tells me he has invited you to Gordon Conference. I hope you come.
with fond regards, Gobind.
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